Canonical Allele Identifier: CA2213422658

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23629883T= , CM000678.2:g.23629883T=	GRCh38
NC_000016.9:g.23641204T= , CM000678.1:g.23641204T=	GRCh37
NC_000016.8:g.23548705T=	NCBI36
NG_007406.1:g.16475A= , LRG_308:g.16475A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.2277A=	ENSP00000460666.3:p.Thr759=
ENST00000565038.2:c.212-608A=	ENSP00000459882.2:n.212-608A=
ENST00000566069.6:c.2271A=	ENSP00000459237.2:p.Thr757=
ENST00000697377.2:c.2277A=	ENSP00000513286.2:p.Thr759=
ENST00000697379.2:c.2277A=	ENSP00000513287.2:p.Thr759=
ENST00000561514.2:c.1386A=	ENSP00000460666.2:p.Thr462=
ENST00000697374.1:c.1386A=	ENSP00000513284.1:p.Thr462=
ENST00000697375.1:n.3618A=
ENST00000697376.1:c.1386A=	ENSP00000513285.1:p.Thr462=
ENST00000697377.1:c.1386A=	ENSP00000513286.1:p.Thr462=
ENST00000697378.1:n.2791A=
ENST00000697379.1:c.1386A=	ENSP00000513287.1:p.Thr462=
ENST00000697380.1:n.1199A=
ENST00000697381.1:n.966A=
ENST00000697382.1:c.1386A=	ENSP00000513288.1:p.Thr462=
ENST00000697383.1:c.49-608A=	ENSP00000513289.1:n.49-608A=
ENST00000697384.1:n.2425A=
ENST00000261584.9:c.2271A= MANE Select	ENSP00000261584.4:p.Thr757=
ENST00000261584.8:c.2271A=	ENSP00000261584.4:p.Thr757=
ENST00000565038.1:c.87-608A=
ENST00000568219.5:c.1386A=	ENSP00000454703.2:p.Thr462=
NM_024675.3:c.2271A= , LRG_308t1:c.2271A=	NP_078951.2:p.Thr757=
XM_011545946.1:c.2277A=	XP_011544248.1:p.Thr759=
XM_011545947.1:c.2277A=	XP_011544249.1:p.Thr759=
XM_011545948.1:c.1386A=	XP_011544250.1:p.Thr462=
XR_950851.1:n.3067A=
XM_011545946.2:c.2277A=	XP_011544248.1:p.Thr759=
XM_011545947.2:c.2277A=	XP_011544249.1:p.Thr759=
XM_011545948.2:c.1386A=	XP_011544250.1:p.Thr462=
XM_017023671.1:c.2277A=	XP_016879160.1:p.Thr759=
XM_017023672.2:c.2271A=	XP_016879161.1:p.Thr757=
XM_017023673.2:c.2271A=	XP_016879162.1:p.Thr757=
NM_024675.4:c.2271A= MANE Select	NP_078951.2:p.Thr757=